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Symbol Name ID |
Aldh3a2
aldehyde dehydrogenase family 3, subfamily A2 MGI:1353452 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Photophobia |
Spasticity |
Spastic paraparesis |
Spastic diplegia |
CNS demyelination |
Abnormal pyramidal sign |
Abnormality of speech or vocalization |
Dysarthria |
Intellectual disability |
Seizure |
| Disease(s) Associated with ALDH3A2 | |||||||||||
| Sjogren-Larsson syndrome |
| Mouse Phenotypes | decreased prepulse inhibition |
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| Availability | Mouse Genotype | |
| Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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